A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999325



Internal ID18812175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83783169..84000144hg38UCSC Ensembl
Innerchr3:83832320..84049295hg19UCSC Ensembl
Innerchr3:83915010..84131985hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38216976
hg19216976
hg18216976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596252
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999325
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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